One step process for regioselective synthesis of alpha-acyloxy carbonyls

ABSTRACT

A regioselective N-Heterocyclic Carbene (NHC) catalyzed one step process for high yield synthesis of α-acyloxy carbonyl compounds is disclosed.

FIELD OF THE INVENTION

The present invention relates to a regioselective one step process for synthesis of α-acyloxy carbonyl compounds. Particularly, present invention discloses a regioselective one step process for synthesis of α-acyloxy carbonyl compounds from alkenes.

BACKGROUND AND PRIOR ART OF THE INVENTION

α-acyloxy carbonyls are often found as the key structural motif for many natural products with interesting biological activities and synthetic therapeutics, refer. P. A. Levine, A. Walti, Org. Synth. Coll. Vol. II 1943, 5. These compounds are the potential starting materials for the pfitzinzer reaction in the synthesis of quinoline salicylic acids and their further functionalization results in various biologically active natural products. The acyl groups can serve as useful protecting groups for the hydroxyl functions in α-hydroxy carbonyls. Their importance is reflected in the extensive synthetic research directed toward introducing acyloxy group in a chemo, regio, stereo and enantioselective manner.

U.S. Pat. No. 6,384,265 discloses method for stereoselectively producing an alpha-acyloxy carbonyl compound from an enol ester epoxide comprising contacting the enol ester epoxide With a chiral acid catalyst under conditions sufficient to stereoselectively produce the alpha-acyloxy carbonyl compound With inversion of stereochemistry.

US 2003/0083376 discloses depot preparations comprising at least one compound of the formula given below.

in which R1, R3 and R4, independently of one another, are an organic radical having 1 to 30 carbon atoms; R2 is hydrogen or an organic radical having 1 to 30 carbon atoms, and the compound of the formula given above, after hydrolysis or enzymatic cleavage, releases an alcohol and a carboxylic acid in addition to the aldehyde or ketone.

U.S. Pat. No. 5,084,584 discloses a process for producing an a-acyloxy-a, β unsaturated carbonyl comprising bringing a propargyl ester into contact with a platinum group metal compound catalyst in the presence of oxygen and/or a peroxide.

U.S. Pat. No. 8,143,423 discloses a process for preparing hydroxamic acids. The process comprises reacting an aldehyde with a nitroso compound in the presence of a N-heterocyclic carbene (NHC) catalyst.

Prior art processes for synthesis of α-acyloxy carbonyls are catalysed by metals, including the direct oxidative coupling of carbonyl compounds with toxic heavy metal oxidants namely Pb(OAc)₄, Tl(OAc)₃, Mn(OAc)₃, thus providing environmentally unfriendly processes.

Some processes replaced heavy metal salts with stoichiometric use of N-methyl-Oacylhydroxylamines, but preparation of N-methyl-Oacylhydroxylamines is not an easy process, Also, this is needed in stoichiometric quantities to lead to the desired α-acyloxy carbonyls. Other prior art processes use harsh conditions for synthesis of desired compounds, making them both economically and environmentally non friendly. Some reports indicate the use of halo substituted carbonyls ie α-halo carbonyls as tarting materials, which are not commercially available, and therefore will have to be synthesized. This results in long evolving methods of synthesis of desired compounds.

Thus there is a need in the art to provide a simple, environmentally friendly process for synthesis of α-acyloxy carbonyls, such that the process provides a high degree of regio selectivity.

OBJECTS OF THE INVENTION

Main objective of the present invention is to provide a one step, one pot process for synthesis of α-acyloxy carbonyls.

Another objective of the invention is to provide a one step, one pot process for synthesis of α-acyloxy carbonyls with high degree of regio selectivity.

Yet another objective of the present invention is to provide an environmentally friendly process conducted in mild conditions with easily available starting compounds.

BRIEF DESCRIPTION OF THE DRAWING

Scheme 1 represents NFIC catalyzed oxidative functionalization of alkenes with aldehydes for synthesis of α-acyloxy carbonyls.

SUMMARY OF THE INVENTION

Accordingly, present invention provides a single-step, one pot process for preparation of α-acyloxy carbonyl compound of general formula (I)

wherein R is selected from H, alkyl, aryl, Bn; R¹ is selected from H, alkyl, substituted aryl, unsubstituted aryl —CH₂OTBS (TBS=Tertiary butyl silyl), —CH₂OBn, —OR, OMOM (Methoxy methelene); Ar is selected from substituted aromatic, unsubstituted aromatic or heteroaromatic; R and R1 optionally can combine to form a ring structure; comprising the steps of:

i. reacting alkene of formula (III) with an aldehyde of formula (IV)

in the presence of a N-Heterocyclic carbene catalyst (NHC), a halogen source, tri-ethyl amine and a solvent in oxygen atmosphere at a temperature in the range of 15-30° C. by stirring for period in the range of 10-50 hours to obtain compound of general formula (I);

wherein R is selected from H, alkyl, aryl, Bn; R¹ is selected from H, alkyl, substituted aryl, unsubstituted aryl —CH₂OTBS (TBS=Tertiary butyl silyl), —CH₂OBn, —OR, OMOM (Methoxy methelene); Ar is selected from substituted aromatic, unsubstituted aromatic or heteroaromatic.

In an embodiment of the present invention, N-Heterocyclic carbene catalyst is selected from the group consisting of IVa-IVf, preferably IVa.

wherein for IVb, Ar=2,4,6-(CH₃)₃C₆H₂; for IVc, Ar=2,6-iPr₂C₆H₃

In another embodiment of the present invention, halogen source is selected from the group consisting of N-bromo succinamide (NBS), N-iodo succinamide NIS or N-chloro succinamide NCS, preferably NBS.

In yet another embodiment of the present invention, solvent used is di-methyl sulfoxide (DMSO).

In yet another embodiment of the present invention, yield of the compound of general formula 1 is in the range of 70 to 42%.

In yet another embodiment of the present invention, representative compound of general formula I are:

-   2-Oxo-2-phenylethyl 4-nitrobenzoate (Ia); -   2-(4-Methylphenyl)-2-oxoethyl 4-nitrobenzoate (Ib); -   2-(4-Bromophenyl)-2-oxoethyl 4-nitrobenzoate (Ic); -   2-(4-Fluorophenyl)-2-oxoethyl 4-nitrobenzoate (Id); -   2-(4-Acetoxyphenyl)-2-oxoethyl 4-nitrobenzoate (le); -   2-(3,4 Dimethoxyphenyl)-2-oxoethyl 4-nitrobenzoate (If); -   1-Oxo-2,3-dihydro-1H-inden-2-yl 4-nitrobenzoate (Ig); -   2-Oxo-1,2-diphenylethyl 4-nitrobenzoate (Ih); -   1-Oxo-1-phenylpropan-2-yl 4-nitrobenzoate (Ii); -   3-((Tert-butyldimethylsilyl)oxy)-1-oxo-1-phenylpropan-2-yl 4-nitro     benzoate (Ij); -   3-(Benzyloxy)-2-oxopropyl 4-nitrobenzoate (Ik); -   2-Oxooctyl 4-nitrobenzoate (Il); -   2-Oxodecyl 4-nitrobenzoate (Im); -   RMD/NEH/CSIR-49 -   2-Oxo-4-phenylbutyl 4-nitrobenzoate (In); -   2-Ethoxy-2-oxoethyl 4-nitrobenzoate (Io); -   2-Oxotetrahydro-2H-pyran-3-yl 4-nitrobenzoate (Ip); -   2-(Methoxy)-2-oxo-1-phenylethyl 4-nitrobenzoate (Iq); -   2-Oxo-2-phenylethyl benzoate (Ir); -   2-Oxo-2-phenylethyl 3-methylbenzoate (Is); -   2-Oxo-2-phenylethyl 4-bromobenzoate (It); -   2-Oxo-2-phenylethyl 4-chlorobenzoate (Iu); -   2-Oxo-2-phenylethyl nicotinate (Iv).

DETAILED DESCRIPTION OF THE INVENTION

Present invention provides a one step, one pot process for the synthesis of α-acyloxy carbonyl compounds with regio selectivity, wherein the starting material is an alkene.

The process leads to novel α-acyloxy carbonyl compounds that may be used as key structural motif for synthesis of useful, therapeutically active compounds.

The present invention provides a single-step, one pot process for the preparation of α-acyloxy carbonyl compounds of general formula (I)

General Formula I

wherein R=H, alkyl, aryl or Bn; R¹═H, alkyl, aryl, —CH₂OTBS, —CH₂OBn, —OR or OMOM; Ar=aromatic or heteroaromatic; comprising reacting alkene of formula (II), with an aldehyde of formula (III)

wherein, R, R1, Ar are as defined above; in the presence of a NHC catalyst, a halogen source, triethyl amine and a solvent selected from di-methyl sulfoxide (DMSO) in air at temperature 15-30° C. by stirring for 10-50 hours and isolating compounds of general formula (I) with >70% yields. N-Heterocyclic carbene catalyst is selected from:

wherein, Vb is Ar=2,4,6-(CH₃)₃C₆H₂; Vc is Ar=2,6-iPr₂C₆H₃.

Halogen source is selected from N-bromo succinamide (NBS), N-iodo succinamide (NIS) or N-chloro succinamide (NCS) and preferably NBS.

The above process for the preparation of α-acyloxy carbonyl compounds of formula (I), using IVa as NHC— catalyst is depicted below in Scheme 1.

The present invention provides a process with variations of the NHC catalyst IVa-IVf yielding the corresponding α-acyloxy carbonyl starting from styrene and —NO₂-benzaldehyde as shown in Table 1.

TABLE 1 NHC catalyzed oxidative functionalization of styrene with 4-NO₂-benzaldehyde: Optimization studies Yield (%)^(b) Entry NHC catalyst Base Solvent of Ia 1 IVa Et₃N DMSO 92 (81)^(c) (46)^(d) 2 IVb Et₃N DMSO 65 3 IVc Et₃N DMSO 47 4 IVd Et₃N DMSO 52 5 IVe Et₃N DMSO 14 6 IVf Et₃N DMSO  8 7 IVa NaH DMSO 54 8 IVa DBU DMSO 52 9 IVa Cs₂CO₃ DMSO 24 10 IVa KOBu^(t) DMSO 16 11 IVa Et₃N DMSO (5 eq) + THF 15 ^(a)Reaction conditions: styrene (5 mmol), p-nitrobenzaldehyde (6 mmol), NHC precatalyst (Va-f) (10 mol %), Base (6 mmol), NBS (5 mmol); all under O₂ atmosphere in DMSO, 25° C., 18 h; ^(b)isolated yield after column chromatographic purification; ^(c)NIS is used instead of NBS; ^(d)NCS is used us halogen source. a: Reaction conditions: styrene (5 mmol), p-nitrobenzaldehyde (6 mmol), NHC precatalyst (Va-1) (10 mol %), Base (6 mmol), NBS (5 mmol); all under O₂ atmosphere in DMSO, 25° C., 18 h; b: isolated yield after column chromatographic purification; c: NIS is used instead of NBS; d: NCS is used us halogen source.

The present invention provides a process for the preparation of α-acyloxy carbonyl compounds of formula (II), wherein the NHC catalysts is preferably IVa to IVd with yields greater than 50%.

The present invention provides a process with options of aldehydes to provide α-acyloxy carbonyl with high regioselectivity yield greater than 70% as shown in Table 2.

TABLE 2 NHC catalyzed oxidative functionalization of styrene with aromatic aldehydes^(a) Time Products Yield (%)^(b) Entry Aldehydes (IIIa-e) (h) (Ir-v) of (Ir-v) 1 benzaldehyde (IIIa) 38 Ir 68 2 m-tolualdehyde (IIIb) 28 Is 81 3 4-Br-benzaldehyde (IIIc) 22 It 78 4 4-Cl-benzaldehyde (IIId) 24 Iu 75 5 3-pyridine carboxaldehyde (IIIe) 22 Iv 73 ^(a)Reaction conditions: styrene (5 m.mol), aromaticaldehyde (5.5 mmol), NHC precatalyst Va (10 mol %), Et₃N (5.5 mmol), NBS (5 mmol) in DMSO under O₂ atmosphere; 25° C.; ^(b)isolated yield after column chromatographic purification.

The present invention provides various α-acyloxy carbonyls synthesized by varying the alkenes (III), with >70% yield as shown in Table 3.

TABLE 3 NHC catalyzed oxidative functionalization of alkenes with 4-NO₂-benzaldehyde^(a) time products entry alkenes (IIa-q) (h) (Ia-q) yield (%)^(b) 1 styrene (IIa) 18 Ia 92 2 4-CH₃-styrene (IIb) 20 Ib 77 3 4-Br-styrene (IIc) 18 Ic 71 4 4-F-styrene (IId) 22 Id 79 5 4-OAc-styrene (IIe) 23 Ie 82 6 3,4-(OMe)₂ styrene (IIf) 26 If 74 7 indene (IIg) 18 Ii 72 8 stilbene (IIh) 24 Ij 81 9 Ph—CH═CH—CH₂—OTBS (IIi) 28 Ig 92 10 3,4-(O—CH₂—O)—Ph—CH═CH—CH₂—OTBS (IIj) 26 Ih 81 11 benzyloxy 1-propene (IIk) 27 Ik 79 12 1-octene (IIl) 32 Il 71 13 1-decene (IIm) 29 Im 76 14 4-phenyl-1-butene (IIn) 26 In 74 15 ethoxyethene (IIo) 30 Io  78^(c) 16 dihydropyran (IIp) 28 Ip 69 17 Ph—CH₂—CH═CH—OCH₂OCH₃ (IIq) 32 Iq 73 ^(a)Reaction conditions: alkene (5 mmol), p-nitrobenzaldehyde (5.5 mmol), NHC precatalyst IVa (10 mol %), Et₃N (5.5 mmol), NBS (5 mmol) in DMSO under O₂ atmosphere; 25° C.; ^(b)isolated yield after column chromatographic purification; ^(c)reaction was carried out at 0° C.

EXAMPLES

Following examples are given by way of illustration therefore should not be construed to limit the scope of the invention.

Example 1 General Experimental Procedure

To a solution of alkenes (IIIa-q) (1 equiv.) in DMSO (20 ml), N-Heterocyclic carbene (10 mol %), N-Bromo succinamide (1 equiv.), triethyl amine (1.2 equiv.) and aldehyde (IVa-f) were added under oxygen atmosphere. The reaction mixture was then stirred at 25° C. After completion (monitored by TLC), the reaction mixture was then concentrated, followed by the addition of H₂O (50 mL). It was extracted with EtOAc (3×50 ml) and the combined organic layers dried over anhydrous Na₂SO₄. Removal of solvent gave α-acyloxy carbonyls (Ia-v), which were purified by column chromatography over silica gel using pet ether/EtOAc (1/19) as eluent to obtain pure α-acyloxy carbonyls in high purity.

Example 2 2-Oxo-2-phenylethyl 4-nitrobenzoate (IIa)

Yield: 92%, colorless solid, Mp: 123-124° C.; IR (Nujol, cm⁻¹): 719, 1104, 1229, 1294, 1376, 1462, 1524, 1598, 1696, 1727, 275, 2840, 2923; ¹H NMR (200 MHz, CDCl₃): δ 5.64 (s, 2H), 7.51-7.55 (m, 2H), 7.63-7.65 (m, 1H), 7.97 (d, J=8.5 Hz, 211), 8.33 (s, 4H); ¹³C NMR (50 MHz, CDCl₃): δ 66.9, 123.4, 127.7, 128.9, 130.9, 133.8, 134.0, 134.7, 150.6, 164.0, 191.0: HRMS (ESI): [M+H]⁺ calcd for C₁₅H₁₁NO₅+H: 286.0715. found: 286.0726.

2-(4-Methylphenyl)-2-oxoethyl 4-nitrobenzoate (IIb)

Yield: 77%, colorless solid, Mp: 114-115° C.; IR (Nujol, cm⁻¹): 713, 1135, 1231, 1289, 1374, 1459, 1525, 1604, 1692, 1725, 2840, 2923; ¹H NMR (200 MHz, CDCl₃): δ 2.46 (s, 3H), 5.62 (s, 2H), 7.32 (d, J=8.1 Hz, 2H), 7.87 (d, J=8.1 Hz, 2H), 8.33 (s, 4H); ¹³C NMR (50 MHz, CDCl₃): δ 21.8, 66.9, 123.5, 127.8, 129.6, 131.1, 131.5, 134.8, 145.1, 150.7, 164.1, 190.6; HRMS (ESI): [M+H]⁺ calcd for: C₁₆H₁₃NO₅+H: 300.0872. found: 300.0881.

2-(4-Bromophenyl)-2-oxoethyl 4-nitrobenzoate (IIc)

Yield: 71%, colorless solid, Mp: 117-118° C.; IR (CHCl₃, cm⁻¹): 717, 967, 1106, 1124, 1346, 1521, 1701, 1723, 2850, 2920; ¹H NMR (200 MHz, CDCl₃): δ 5.58 (s, 2H), 7.67 (m, J=8.5 Hz, 2H), 7.83 (m, J 8.5 Hz, 2H), 8.32 (s, 4H); ¹³C NMR (100 MHz, CDCl₃): δ 66.7, 123.6, 129.2, 129.5, 131.1, 132.4, 132.6, 134.6, 150.8, 164.0, 190.0; HRMS (ESI): [M+H]⁺ calcd for C₁₅H₁₀BrNNaO₅+H: 363.9820. found: 363.9834.

2-(4-Fluorophenyl)-2-oxoethyl 4-nitrobenzoate (IId)

Yield: 79%, colorless solid, Mp: 117-118° C.; IR (CHCl₃, cm⁻¹): 717, 871, 1131, 1155, 1231, 1320, 1521, 1595, 1698, 1722, 1746; ¹H NMR (400 MHz, CDCl₃): δ 5.59 (s, 2H), 7.21 (t, J=8.6 Hz, 2H), 8.01 (dd, J=8.6, J=5.0 Hz, 2H), 8.32 (d, J=2.7 Hz, 4H); ¹³C NMR (100 MHz, CDCl₃): δ 66.7, 116.1, 116.4, 130.5, 130.5, 131.1, 134.6, 150.8, 164.0, 165.0, 167.5, 189.3; HRMS (ESI): [M+H]⁺ calcd for C₁₅H₁₀FNO₅+H: 304.0621. found: 304.0627.

2-(4-Acetoxyphenyl)-2-oxoethyl 4-nitrobenzoate (IIe)

Yield: 82%, colorless solid, Mp: 128-129° C.; IR (Nujol, cm⁻¹): 716, 1166, 1212, 1294, 1374, 1459, 1525, 1596, 1690, 1717, 1753, 2846, 2917; ¹H NMR (200 MHz, CDCl₃): δ 2.35 (s, 3H), 5.61 (s, 2H), 7.26 (d, J=8.6 Hz, 2H), 8.01 (d, J=8.6 Hz, 2H), 8.32 (s, 4H); ¹³C NMR (100 MHz, CDCl₃): δ 21.0, 66.7, 122.2, 123.5, 129.3, 131.0, 131.3, 134.6, 150.6, 155.0, 164.0, 168.4, 189.9; FIRMS (ESI): [M+H]⁺ calcd for C₁₇H₁₃NO₇+H: 344.0770. found: 344.0778.

2-(3,4 Dimethoxyphenyl)-2-oxoethyl 4-nitrobenzoate (IIf)

Yield: 74%, colorless solid, Mp: 162-163° C.; IR (Nujol, cm⁻¹): 720, 1021, 1131, 1235, 1376, 1460, 1524, 1684, 1725, 2855, 2925; ¹H NMR (200 MHz, CDCl₃): δ 3.95 (s, 3H), 3.98 (s, 311), 5.60 (s, 2H), 6.92 (d, J=8.3 Hz, 1H), 7.51-7.54 (m, 2H), 8.33 (s, 4H); ¹³C NMR (100 MHz, CDCl₃): δ 55.9, 56.0, 66.6, 110.0, 110.1, 122.1, 123.6, 127.1, 131.0, 134.9, 149.5, 150.8, 154.1, 164.1, 189.5; HRMS (ESI): [M+H]⁺ calcd for C₁₇H₁₅NO₇+H: 346.0922. found: 346.0927.

1-Oxo-2,3-dihydro-1H-inden-2-yl 4-nitrobenzoate (IIg)

Yield: 72%, colorless solid, Mp: 199-200° C.; IR (Nujol, cm⁻¹): 713, 1122, 1273, 1349, 1374, 1522, 1604, 1709, 1722, 2846, 2923; ¹H NMR (200 MHz, CDCl₃): δ 3.23 (dd, J=17.0, 4.9 Hz, 1H), 3.82 (dd, J=17.0, 8.1 Hz, 1H), 5.70 (dd, J=8.1, 4.9 Hz, 1H), 7.44-7.53 (m, 2H), 7.68 (d, J 7.7 Hz, 1H), 7.86 (d, J 7.7 Hz, 1H), 8.30 (s, 4H); ¹³C NMR (125 MHz, CDCl₃): δ 33.4, 75.0, 123.6, 124.7, 126.7, 128.4, 131.1, 134.5, 134.7, 136.1, 150.1, 150.9, 164.1, 199.3; HRMS (ESI): [M+H]⁺ calcd for: C₁₆H₁₂NO₅+H: 298.0715. found: 298.0720.

2-Oxo-1,2-diphenylethyl 4-nitrobenzoate (IIh)

Yield: 81%, colorless solid, Mp: 114-115° C.; IR (Nujol, cm⁻¹): 762, 1097, 1288, 1341, 1374, 1462, 1522, 1692, 1720, 2851, 2923; ¹H NMR (200 MHz, CDCl₃): δ 7.13 (s, 111), 7.41-7.58 (m, 8H), 7.99 (d, J=7.2 Hz, 2H), 8.28 (s, 4H); ¹³C NMR (50 MHz, CDCl₃): δ 78.7, 123.5, 128.7, 128.8, 129.3, 129.7, 131.1, 133.2, 133.6, 134.4, 134.8, 150.7, 164.0, 192.6: HRMS (ESI): [M+Na]⁺ calcd for: C₂₁H₁₅NO₅+Na: 384.0848. found: 384.0853.

1-Oxo-1-phenylpropan-2-yl 4-nitrobenzoate (IIi)

Yield: 81%, colorless solid, Mp: 119-120° C.; IR (Nujol, cm⁻¹): 721, 965, 1122, 1270, 1374, 1462, 1522, 1599, 1692, 1725, 2851, 2923; ¹H NMR (200 MHz, CDCl₃): δ 1.72 (d, J=6.9 Hz, 3H), 6.23 (q, 0.1=6.9 Hz, 1H), 7.52-7.63 (m, 3H), 7.97-8.01 (m, 211), 8.29-8.30 (m, 4H); ¹³C NMR (100 MHz, CDCl₃); δ 17.2, 72.6, 123.4, 128.4, 128.8, 130.9, 133.7, 134.8, 150.6, 163.9, 195.5; HRMS (ESI): [M+H]⁺ calcd for: C₁₆H₁₃NO₅+H: 300.0872. found: 300.0877.

3-((Tert-butyldimethylsilyl)oxy)-1-oxo-1-phenylpropan-2-yl 4-nitro benzoate (IIj)

Yield: 92%, colorless solid, Mp: 77-78° C.; IR (Nujol, cm⁻¹): 718, 839, 1270, 1371, 1459, 1530, 1695, 1733, 2851, 2917; ¹H NMR (200 MHz, CDCl₃): δ 0.00 (s, 3H), 0.02 (s, 3H), 0.82 (s, 9H), 4.18 (d, J=5.1 Hz, 2H), 6.25 (t, J=5.1 Hz, 111), 7.47-7.62 (m, 3H), 8.00-8.04 (m, 2H), 8.29-8.30 (m, 4H); ¹³C NMR (100 MHz, CDCl₃): δ −5.4, 18.1, 25.6, 29.7, 62.9, 77.3, 123.5, 128.5, 128.7, 131.0, 133.7, 134.8, 135.2, 150.7, 163.9, 194.4; HRMS (ESI): [M+H]⁺ calcd for: C₂₂H₂₇NO₆Si+H: 430.1686. found: 430.1689.

3-(Benzyloxy)-2-oxopropyl 4-nitrobenzoate (IIk)

Yield: 79%, colorless solid, Mp: 83-84° C.; IR (Nujol, cm⁻¹): 718, 1083, 1283, 1374, 1459, 1517, 1722, 1739, 2851, 2823; ¹H NMR (200 MHz, CDCl₃): δ 4.21 (s, 2H), 4.64 (s, 2H), 5.23 (s, 2H), 7.37 (s, 5H), 8.28 (d, J=4.3 Hz, 4H); ¹³C NMR (125 MHz, CDCl₃): δ 67.8, 73.8, 73.9, 123.5, 127.9, 128.3, 128.6, 130.9, 134.6, 136.5, 150.7, 163.8, 200.8; HRMS (ESI): [M+Na]⁺ calcd for C₁₇H₁₅NO₆+Na: 352.0796. found: 352.0801.

2-Oxooctyl 4-nitrobenzoate (IIl)

Yield: 71%, colorless solid, Mp: 75-76° C.: IR (Nujol, cm⁻¹): 717, 1121, 1272, 1352, 1377, 1463, 1536, 1543, 1722, 1733, 2854, 2923; ¹H NMR (200 MHz, CDCl₃): δ 0.87-0.93 (m, 3H), 1.26-1.31 (br. s, 6H), 1.67-1.70 (m, 2H), 2.49 (t, J=7.3 Hz, 2H), 4.94 (s, 2H), 8.24-8.35 (m, 4H); ¹³C NMR (125 MHz, CDCl₃): δ 13.9, 22.4, 23.2, 28.7, 31.5, 38.7, 68.7, 123.5, 130.9, 134.6, 150.7, 163.8, 202.4: HRMS (ESI): [M+H]⁺ calcd for C₁₅H₁₉NO₅+H: 294.1341. found: 294.1347.

2-Oxodecyl 4-nitrobenzoate (IIm)

Yield: 76%, colorless solid, Mp: 76-77° C.; IR (Nujol, cm⁻¹): 713, 1119, 1270, 1374, 1459, 1541, 1610, 1717, 1736, 2857, 2928; ¹H NMR (200 MHz, CDCl₃): δ 0.85-0.92 (m, 3H), 1.29 (br. s., 10H), 1.66 (t, J=7.2 Hz, 2H), 2.49 (t, J=7.2 Hz, 2H), 4.94 (s, 2H), 8.24-8.35 (m, 4H); ¹³C NMR (50 MHz, CDCl₃): δ 14.0, 22.5, 23.2, 29.0, 29.0, 29.2, 31.7, 38.6, 68.6, 123.4, 130.8, 134.6, 150.6, 163.7, 202.2; HRMS (ESI): [M+H]⁺ calcd for C₁₇H₂₃NO₅+H: 322.1654. found: 322.1656.

2-Oxo-4-phenylbutyl 4-nitrobenzoate (IIn)

Yield: 74%, colorless solid, Mp: 112-113° C.; IR (Nujol, cm⁻¹): 724, 1089, 1131, 1273, 1347, 1377, 1462, 1523, 1600, 1718, 1732, 2855, 2926; ¹H NMR (200 MHz, CDCl₃): δ 2.79-2.87 (m, 211), 2.95-3.03 (m, 211), 4.91 (s, 2H), 7.21-7.31 (m, 511), 8.27-8.34 (m, 4H); ¹³C NMR (50 MHz, CDCl₃): δ 29.2, 40.4, 68.8, 123.6, 126.4, 128.2, 128.6, 131.0, 138.0, 140.2, 150.8, 163.9, 201.7; HRMS [M+Na]⁺ calcd for: C₁₇H₁₅NO₅+Na: 336.0848. found: 336.0856.

2-Ethoxy-2-oxoethyl 4-nitrobenzoate (IIo)

Yield: 78%, yellow liquid; IR (neat, cm⁻¹): 2926, 2983, 1759, 1738, 1732, 1608, 1531, 1349, 1285, 1213, 1121, 1018, 857, 718; ¹H NMR (200 MHz, CDCl₃): δ 1.33 (t, J=7.1 Hz, 3H), 4.28 (q, J=7.1 Hz, 2H), 4.89 (s, 2H), 8.25-8.36 (m, 4H); ¹³C NMR (50 MHz, CDCl₃): δ 14.1, 61.5, 123.5, 131.0, 134.5, 150.8, 163.9, 166.9; HRMS (ESI): [M+Na]⁺ calcd for C₁₁H₁₁NO₆+Na: 276.0484. found: 276.0446.

2-Oxotetrahydro-2H-pyran-3-yl 4-nitrobenzoate (IIp)

Yield: 69%, colorless solid, Mp: 136-137° C.; IR (Nujol, cm⁻¹): 718, 1124, 1273, 1377, 1456, 1511, 1602, 1725, 1753, 2857, 2912; ¹H NMR (200 MHz, CDCl₃): δ 2.14-2.20 (m, 3H),

2.51-2.76 (m, 1H), 4.43-4.49 (m, 2H), 5.61-5.67 (m, 1H), 8.25-8.35 (m, 4H); ¹³C NMR (50 MHz, CDCl₃): δ 21.3, 24.8, 68.2, 68.2, 123.5, 131.0, 134.5, 150.7, 163.4, 168.1; HRMS (ESI): [M+H]⁺ calcd for C₁₂H₁₁NO₆+H: 266.0664. found: 266.0663.

2-(Methoxy)-2-oxo-1-phenylethyl 4-nitrobenzoate (IIq)

Yield: 72%, yellow liquid; IR (CHCl₃, cm⁻¹): 718, 1101, 1167, 1269, 1346, 1368, 1508, 1527, 1606, 1731, 1760; ¹H NMR (500 MHz, CDCl₃): δ 3.80 (s, 3H), 6.20 (s, 1H), 7.47-7.48 (m, 3H), 7.59-7.60 (m, 2H), 8.32 (s, 4H); ¹³C NMR (125 MHz, CDCl₃): δ 52.6, 75.4, 123.5, 127.7, 128.9, 129.5, 131.0, 133.3, 134.5, 150.8, 163.7, 168.5; HRMS (ESI): [M+Na]⁺ calcd for C₁₆H₁₃NO₆+Na: 338.0641. found: 338.0649.

2-Oxo-2-phenylethyl benzoate (IIr)

Yield: 68%, colorless solid, Mp: 119-120° C.; IR (Nujol, cm⁻¹): 705, 1015, 1374, 1459, 1596, 1714, 1750, 2851, 2923; ¹H NMR (200 MHz, CDCl₃): δ 5.58 (s, 211), 7.48-7.61 (m, 6H), 7.97-8.00 (m, 2H), 8.13-8.17 (m, 2H); ¹³C NMR (50 MHz, CDCl₃): δ 66.2, 127.6, 128.2, 128.73, 129.8, 130.1, 133.1, 133.6, 134.1, 165.7, 191.6; HRMS (ESI): [M+Na]⁺ calcd for C₁₅H₁₂O₃+Na: 263.0683. found: 263.0692.

2-Oxo-2-phenylethyl 3-methylbenzoate (IIs)

Yield: 81%, colorless solid, Mp: 94-95° C.; IR (Nujol, cm): 743, 814, 957, 1083, 1198, 1369, 1451, 1585, 1684, 1714, 2857, 2917; ¹H NMR (200 MHz, CDCl₃): δ 2.38 (s, 3H), 5.52 (s, 2H), 7.31-7.48 (m, 5H), 7.90-7.95 (m, 4H); ¹³C NMR (100 MHz, CDCl₃): δ 21.1, 66.2, 127.0,

127.6, 128.2 128.7, 129.2, 130.3, 133.6, 133.9, 134.1, 137.9, 165.8, 191.7; HRMS (ESI): [M+Na]⁺ calcd for C₁₆H₁₄O₃+Na: 277.0840. found: 277.0848.

2-Oxo-2-phenylethyl 4-bromobenzoate (IIt)

Yield: 78%, colorless solid, Mp: 84-85° C.; IR (Nujol, cm⁻¹): 766, 1012, 1126, 1327, 1588, 1643, 1711, 1732, 2923, 295′6; ¹H NMR (200 MHz, CDCl₃): δ 5.57 (s, 211), 7.44-7.64 (m, 5H), 7.94-8.03 (m, 4H); ¹³C NMR (50 MHz, CDCl₃): δ 66.4, 127.7, 128.3, 128.4, 128.8, 131.4, 131.7, 133.8, 134.1, 165.0, 191.4: HRMS (ESI): [M+Na]⁺ calcd for C₁₅H₁₁BrO₃+Na: 340.9789. found: 340.9799.

2-Oxo-2-phenylethyl 4-chlorobenzoate (IIu)

Yield: 75%, colorless solid, Mp: 127-128° C.; IR (Nujol, cm⁻¹): 753, 1091, 1226, 1273, 1376, 1456, 1595, 1697, 1726, 2724, 2857, 2926; ¹H NMR (500 MHz, CDCl₃): δ 5.58 (s, 2H) 7.44-7.56 (m, 5H), 7.97 (d, J=7.3 Hz, 2H) 8.07 8.11 (d, J=7.3 Hz, 2H); ¹³C NMR (125 MHz, CDCl₃): δ 66.5, 77.0, 127.8, 128.6, 128.8, 128.9, 131.3, 133.9, 134.2, 139.8, 165.0, 191.6; HRMS (ESI): [M+Na]⁺ calcd for C₁₅H₁₁ClO₃+Na: 297.0294. found: 297.0294.

2-Oxo-2-phenylethyl nicotinate (IIv)

Yield: 73%, colorless solid, Mp: 64-65° C.: IR (CHCl₃, cm⁻¹): 753, 1076, 1342, 1463, 1591, 1650, 1695, 1726, 2854, 2870, 2923; ¹H NMR (400 MHz, CDCl₃); δ 5.61 (s, 214), 7.44 (dd, J=7.6, 4.9 Hz, 1H) 7.50-7.54 (m, 2H), 7.62-7.64 (m, 1H), 7.97 (d, J=7.5 Hz, 2H), 8.40 (d, J=7.7 Hz, 1H), 8.82 (br. s, 1H), 9.33 (br. s, 1H); ¹³C NMR (100 MHz, CDCl₃) δ 66.6,

123.3, 125.6, 127.8, 128.9, 134.0, 134.1, 137.4, 151.2, 153.7, 164.6, 191.1; HRMS (ESI): [M+Na]⁺ calcd for C₁₄H₁₁NO₃+Na: 264.0637. found: 264.0648.

Advantages of the Invention

A new catalytic regio selective method for the preparation of acyloxy carbonyl products in preparative yield from a variety of olefins including aromatic, aliphatic and electron rich at ambient conditions is disclosed. This method is simple, milder and the reagents used are cheap and easy to handle. The process avoids metal catalysts. 

1. A single-step, one pot process for preparation of α-acyloxy carbonyl compound of general formula (I)

wherein R is selected from H, alkyl, aryl, Bn; R¹ is selected from H, alkyl, substituted aryl, unsubstituted aryl —CH₂OTBS (TBS=Tertiary butyl silyl), —CH₂OBn, —OR, OMOM (Methoxy methelene); Ar is selected from substituted aromatic, unsubstituted aromatic or heteroaromatic; R and R1 Optionally can combine to form a ring structure; comprising the steps of: i) reacting alkene of formula (III) with an aldehyde of formula (IV)

in the presence of a N-Heterocyclic carbene catalyst (NHC), a halogen source, tri-ethyl amine and a solvent in oxygen atmosphere at a temperature in the range of 15-30° C. by stirring for period in the range of 10-50 hours to obtain compound of general formula (I); wherein R is selected from H, alkyl, aryl, Bn; R¹ is selected from H, alkyl, substituted aryl, unsubstituted aryl —CH₂OTBS (TBS=Tertiary butyl silyl), —CH₂OBn, —OR, OMOM (Methoxy methelene); Ar is selected from substituted aromatic, unsubstituted aromatic or heteroaromatic.
 2. The process as claimed in, claim 1, wherein N-Heterocyclic carbene catalyst is selected from the group consisting of IVa-IVf, preferably IVa.

Wherein for IVb, Ar=2,4,6-(CH₃)₃C₆H₂; for IVc, Ar=2,6-iPr₂C₆H₃
 3. The process as claimed in claim 1, wherein halogen source is selected from the group consisting of N-bromo succinamide (NBS), N-iodo succinamide NIS or N-chloro succinamide NCS, preferably NBS.
 4. The process as claimed in claim 1, wherein solvent used is di-methyl sulfoxide (DMSO).
 5. The process as claimed in claim 1, wherein yield of the compound of general formula 1 is in the range of 70 to 92%.
 6. The process according to claim 1, wherein representative compound of general formula I are: 2-Oxo-2-phenylethyl 4-nitrobenzoate (Ia); 2-(4-Methylphenyl)-2-oxoethyl 4-nitrobenzoate (Ib); 2-(4-Bromophenyl)-2-oxoethyl 4-nitrobenzoate (Ic); 2-(4-Fluorophenyl)-2-oxoethyl 4-nitrobenzoate (Id); 2-(4-Acetoxyphenyl)-2-oxoethyl 4-nitrobenzoate (Ie); 2-(3,4 Dimethoxyphenyl)-2-oxoethyl 4-nitrobenzoate (If); 1-Oxo-2,3-dihydro-1H-inden-2-yl 4-nitrobenzoate (Ig); 2-Oxo-1,2-diphenylethyl 4-nitrobenzoate (Ih); 1-Oxo-1-phenylpropan-2-yl 4-nitrobenzoate (Ii); 3-((Tert-butyldimethylsilyl)oxy)-1-oxo-1-phenylpropan-2-yl 4-nitro benzoate (Ij); 3-(Benzyloxy)-2-oxopropyl 4-nitrobenzoate (Ik); 2-Oxooctyl 4-nitrobenzoate (II); 2-Oxodecyl 4-nitrobenzoate (Im); 2-Oxo-4-phenylbutyl 4-nitrobenzoate (In); 2-Ethoxy-2-oxoethyl 4-nitrobenzoate (Io); 2-Oxotetrahydro-2H-pyran-3-yl 4-nitrobenzoate (Ip); 2-(Methoxy)-2-oxo-1-phenylethyl 4-nitrobenzoate (Iq); 2-oxo-2-phenylethyl benzoate (Ir); 2-Oxo-2-phenylethyl 3-methylbenzoate (Is); 2-Oxo-2-phenylethyl 4-bromobenzoate (It); 2-Oxo-2-phenylethyl 4-chlorobenzoate (Iu); 2-Oxo-2-phenylethyl nicotinate (Iv). 